EP0549994A2 - Global planarization process - Google Patents
Global planarization process Download PDFInfo
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- EP0549994A2 EP0549994A2 EP92121777A EP92121777A EP0549994A2 EP 0549994 A2 EP0549994 A2 EP 0549994A2 EP 92121777 A EP92121777 A EP 92121777A EP 92121777 A EP92121777 A EP 92121777A EP 0549994 A2 EP0549994 A2 EP 0549994A2
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- Prior art keywords
- layer
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- interlevel dielectric
- substrate
- planarization
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- 238000000034 method Methods 0.000 title claims abstract description 62
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 50
- 238000002844 melting Methods 0.000 claims abstract description 18
- 230000008018 melting Effects 0.000 claims abstract description 18
- 239000004065 semiconductor Substances 0.000 claims abstract description 12
- 238000005229 chemical vapour deposition Methods 0.000 claims abstract description 11
- 238000005240 physical vapour deposition Methods 0.000 claims abstract description 7
- 238000001704 evaporation Methods 0.000 claims abstract description 3
- 230000008020 evaporation Effects 0.000 claims abstract 2
- 238000007747 plating Methods 0.000 claims abstract 2
- 229910052718 tin Inorganic materials 0.000 claims description 48
- 239000000758 substrate Substances 0.000 claims description 17
- 230000004888 barrier function Effects 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 12
- 229910052738 indium Inorganic materials 0.000 claims description 8
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 8
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 7
- 229910052797 bismuth Inorganic materials 0.000 claims description 6
- 238000000151 deposition Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 239000000356 contaminant Substances 0.000 claims description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims 3
- 229910001152 Bi alloy Inorganic materials 0.000 claims 1
- 229910000846 In alloy Inorganic materials 0.000 claims 1
- 229910001128 Sn alloy Inorganic materials 0.000 claims 1
- 239000005380 borophosphosilicate glass Substances 0.000 claims 1
- 238000005234 chemical deposition Methods 0.000 claims 1
- 238000005530 etching Methods 0.000 claims 1
- 238000005289 physical deposition Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 abstract description 21
- 239000002184 metal Substances 0.000 abstract description 21
- 238000009835 boiling Methods 0.000 abstract description 7
- 229910045601 alloy Inorganic materials 0.000 abstract description 6
- 239000000956 alloy Substances 0.000 abstract description 6
- 238000007711 solidification Methods 0.000 abstract description 5
- 238000005498 polishing Methods 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 230000008021 deposition Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000011065 in-situ storage Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 229910052681 coesite Inorganic materials 0.000 description 4
- 229910052906 cristobalite Inorganic materials 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 230000008023 solidification Effects 0.000 description 4
- 238000004544 sputter deposition Methods 0.000 description 4
- 229910052682 stishovite Inorganic materials 0.000 description 4
- 229910052905 tridymite Inorganic materials 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000005137 deposition process Methods 0.000 description 3
- 239000005360 phosphosilicate glass Substances 0.000 description 3
- 238000012876 topography Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000002310 reflectometry Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- KXCAEQNNTZANTK-UHFFFAOYSA-N stannane Chemical compound [SnH4] KXCAEQNNTZANTK-UHFFFAOYSA-N 0.000 description 2
- 229910000083 tin tetrahydride Inorganic materials 0.000 description 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- 229910001361 White metal Inorganic materials 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000013386 optimize process Methods 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 229920005591 polysilicon Polymers 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005389 semiconductor device fabrication Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 239000010969 white metal Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/027—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
- H01L21/0271—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
- H01L21/0273—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers characterised by the treatment of photoresist layers
- H01L21/0274—Photolithographic processes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/31051—Planarisation of the insulating layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/32115—Planarisation
- H01L21/3212—Planarisation by chemical mechanical polishing [CMP]
Definitions
- CMP is the main and until now, the only proven global planarization technique which is being seriously considered for sub-0.5 ⁇ m technologies.
- successful implementations of CMP for semiconductor device manufacturing demands effective post-CMP cleaning process in order to remove the CMP-induced surface contaminants and damage. Much work remains to be done in order to make CMP a fully manufacturable and optimized process.
- Figure 1 is a cross-sectional drawing similar to figure 1, illustrating the etch-back end-point level before melting and resolidification but after deposition.
- Figure 2 is a cross-sectional drawing illustrating the resulting planarized structure up to the sixth processing step (after melting and resolidification).
- Figure 3 illustrates a graph of the surface reflectance R versus time t used for planarization process end-point detection.
- Figure 4 illustrates a graph showing sheet resistance measured in ohms per square versus etch time t which is also useful for planarization process end-point detection.
- Figure 5 is a cross-sectional which illustrates the resulting structure after the etch-back step indicating a globally planarized surface.
- the invention provides a process which is simple to implement, for global planarization of semiconductor chips.
- This process provides true global planarization (e.g. on the lateral scale of 1000's of ⁇ m to several centimeters) and can be used instead of CMP.
- the invention's global planarization process does not employ any mechanical polishing and, as a result, does not require any post-planarization surface cleaning such as the special post-CMP cleaning requirements.
- This invention is fully compatible with existing semiconductor processing equipment.
- this invention is fully compatible with various metallization systems (e.g. Al/SiO2, Cu/SiO2, W/SiO2, Au/SiO2 and etc.) and can be employed before and/or after each metal level in multi-level metal technologies.
- MMSP metal-melt solidification planarization
- This global planarization process can be used to form planarized dielectric, metal, or semiconductor surfaces.
- the process flow to be described here is for dielectric planarization.
- a suggested process flow based on the global planarization of this invention is as follows (assuming a 3-level metal semiconductor technology, although note that technologies with fewer or more levels of metal can suitably be adapted for use with the following process):
- Tin is considered the metal of preferred choice since it meets the melting and boiling point requirements for the planarization layer at melting point temperatures that are not deleterious to conventional metal layers such as aluminium. Restated, the requirements for the planarization layer are that it should melt without evaporating at relatively low temperatures and, therefore, that it have a low vapor pressure at temperatures below 1000°C. Tin is also fairly cheap and abundant. Indium is much more expensive than tin. Bismuth forms low melting point alloys with thin. Bismuth is also fairly cheap.
- tin, indium, bismuth or their alloys can be used for the application of this invention due to their low melting points (below 300°C), high boiling points, and very low vapor pressures below 1000°C. In fact, their vapor pressures are extremely low at less than 500°C.
- the deposition process for the planarization layer can be accomplished by a physical-vapor deposition process (PVD) such as sputtering or it can be accomplished by chemical-vapor deposition (CVD) if a CVD precursor is available.
- PVD physical-vapor deposition
- CVD chemical-vapor deposition
- tin, tin tetrachlorie (SnCl4) and tin hydride (SnH4) may be used as suitable CVD precursors.
- the thickness of a sputtered or evaporated (or CVD-formed) tin planarization layer is selected such that sufficient tin material layer is available to cover the entire nonplanar topography when molten planar tin metal is formed later on. In general, the tin layer thicknesses of 1-4 ⁇ m are sufficiently large to achieve global planarization over semiconductor integrated circuits.
- the barrier layer is not always needed. This is likely the case when tin is used as the disposable planarization layer. Tin is a column IV metal in the periodic table as is silicon the likely semiconductor substrate. Therefore, tin does not act as a generation/recombination (defect) center with respect to a silicon semiconductor substrate. Consequently, the barrier layer can probably be omitted with this planarization layer/substrate combination.
- Figure 1 is a cross-sectional drawing illustrating the resulting structure from the foregoing processing steps. Shown in figure 1 are substrate 2, interlevel dielectric layer 3, adhesion layer 6, barrier layer 4 and planarization layer 8.
- planarization steps tin sputter deposition or tin CVD, wafer heating/tin melting, wafer cooling/ tin solidification, tin etch-back
- tin sputter deposition or tin CVD wafer heating/tin melting
- wafer cooling/ tin solidification wafer cooling/ tin solidification
- tin etch-back the entire sequence of planarization steps can be performed in-situ within a single PVD or CVD chamber.
- the deposition process of the planarization layer can be performed while the wafer is heated to above the melting point of tin (e.g. between 232°C and 400°C). This will result in formation of globally planar tin melt during the deposition. As a result, the two steps of tin deposition and melt resolidification can be performed in a single process step.
- tin melting point
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
- Drying Of Semiconductors (AREA)
- Formation Of Insulating Films (AREA)
Abstract
Description
- Surface planarization is an important requirement for device reliability and depth-of-focus (DOF) requirements of advanced optical lithography tools. Depth-of-focus issues arise when attempting to focus a mask pattern on a surface area with uneven topography. The portion of the surface farther away from the imaging camera lens can be out of focus with respect to the portion of the surface closer to the imaging camera lens or vice versa. As the semiconductor technologies are scaled to sub-0.5 micron (µm) dimensions, improved planarization techniques are required in order to achieve both local and global surface planarization. Local planarization involves planarization over a small portion or lateral scale of an area, while global planarization involves complete planarization over the entire chip area. To date, the following techniques have been proposed or employed for semiconductor device fabrication:
- a) spin-on glass (SOG) and etch-back used for local planarization;
- b) spin- on resist and etch-back (REB) used for local planarization;
- c) in-situ planarized oxide deposition using electron cyclotron resonance, ECR, or plasma used for local planarization;
- d) chemical/mechanical polishing (CMP) used for global planarization;
- e) plasma deposited polymer films plus etch-back (e.g. that used in Lincoln Lab's work on disposable polymer films for local/global planarization); and
- f) phosphosilicate glass (PSG) or borophosposilicate glass (BPSG) reflow used for local planarization.
- CMP is the main and until now, the only proven global planarization technique which is being seriously considered for sub-0.5µm technologies. However, successful implementations of CMP for semiconductor device manufacturing demands effective post-CMP cleaning process in order to remove the CMP-induced surface contaminants and damage. Much work remains to be done in order to make CMP a fully manufacturable and optimized process.
- Figure 1 is a cross-sectional drawing similar to figure 1, illustrating the etch-back end-point level before melting and resolidification but after deposition.
- Figure 2 is a cross-sectional drawing illustrating the resulting planarized structure up to the sixth processing step (after melting and resolidification).
- Figure 3 illustrates a graph of the surface reflectance R versus time t used for planarization process end-point detection.
- Figure 4 illustrates a graph showing sheet resistance measured in ohms per square versus etch time t which is also useful for planarization process end-point detection.
- Figure 5 is a cross-sectional which illustrates the resulting structure after the etch-back step indicating a globally planarized surface.
- Reference numerals in the figures are carried forward.
- The invention provides a process which is simple to implement, for global planarization of semiconductor chips. This process provides true global planarization (e.g. on the lateral scale of 1000's of µm to several centimeters) and can be used instead of CMP. The invention's global planarization process does not employ any mechanical polishing and, as a result, does not require any post-planarization surface cleaning such as the special post-CMP cleaning requirements. This invention is fully compatible with existing semiconductor processing equipment. Moreover, this invention is fully compatible with various metallization systems (e.g. Al/SiO₂, Cu/SiO₂, W/SiO₂, Au/SiO₂ and etc.) and can be employed before and/or after each metal level in multi-level metal technologies. The disclosed process can be appropriately called metal-melt solidification planarization (MMSP). This global planarization process can be used to form planarized dielectric, metal, or semiconductor surfaces. The process flow to be described here is for dielectric planarization. A suggested process flow based on the global planarization of this invention is as follows (assuming a 3-level metal semiconductor technology, although note that technologies with fewer or more levels of metal can suitably be adapted for use with the following process):
- 1) Complete the device fabrication process flow on a semiconductor wafer through all the steps for fabrication of the active devices. In other words complete the fabrication flow up to a point just prior to the first metal level.
- 2) Deposit the first interlevel dielectric (ILD) 3 such as PSG or BPSG or undoped oxide (or a stacked combination thereof).
- 3) Deposit a thin (approximately 400-1000Å) of a diffused
barrier layer 4 such as plasma deposited silicon nitride. This layer is optional depending upon the type of disposable planarization layer used as will be explained further. The barrier layer will act as a diffusion barrier and is disposable. The barrier layer prevents diffusion of the disposable planarization layer atoms into the substrate on which the active devices lie. - 4) Deposit a thin (approximately 400-1000Å) buffer/adhesion or
glue layer 8 of a suitable material, which serves to both adhere to the planarization layer (a layer explained below) and act as a barrier from contamination of the substrate by the planarization layer. Suitable material for the buffer/adhesion layer includes materials such as polysilicon, titanium, aluminium or their alloys. This can be done using physical-vapor deposition (PVD) such as sputtering or this can be done using chemical-vapor deposition (CVD). Other adhesion or glue layer mateials may be used. - 5) Deposit a relatively thick layer (e.g. a layer 1µm to a few microns thick) of a low melting point (a low melting point being considered below 400°C) and high boiling point (a high boiling point being considered above 1500°C) elemental metal or suitable alloy. This relatively thick layer shall serve as a disposable planarization layer. Tin, indium and bismuth are considered suitable materials as shown below in table A which indicates melting point and boiling point temperatures at atmospheric pressure in Celsius.
- Tin is considered the metal of preferred choice since it meets the melting and boiling point requirements for the planarization layer at melting point temperatures that are not deleterious to conventional metal layers such as aluminium. Restated, the requirements for the planarization layer are that it should melt without evaporating at relatively low temperatures and, therefore, that it have a low vapor pressure at temperatures below 1000°C. Tin is also fairly cheap and abundant. Indium is much more expensive than tin. Bismuth forms low melting point alloys with thin. Bismuth is also fairly cheap.
- In general, tin, indium, bismuth or their alloys can be used for the application of this invention due to their low melting points (below 300°C), high boiling points, and very low vapor pressures below 1000°C. In fact, their vapor pressures are extremely low at less than 500°C.
- The deposition process for the planarization layer can be accomplished by a physical-vapor deposition process (PVD) such as sputtering or it can be accomplished by chemical-vapor deposition (CVD) if a CVD precursor is available. For tin, tin tetrachlorie (SnCl₄) and tin hydride (SnH₄) may be used as suitable CVD precursors. The thickness of a sputtered or evaporated (or CVD-formed) tin planarization layer is selected such that sufficient tin material layer is available to cover the entire nonplanar topography when molten planar tin metal is formed later on. In general, the tin layer thicknesses of 1-4 µm are sufficiently large to achieve global planarization over semiconductor integrated circuits.
- As indicated above the barrier layer is not always needed. This is likely the case when tin is used as the disposable planarization layer. Tin is a column IV metal in the periodic table as is silicon the likely semiconductor substrate. Therefore, tin does not act as a generation/recombination (defect) center with respect to a silicon semiconductor substrate. Consequently, the barrier layer can probably be omitted with this planarization layer/substrate combination.
- Figure 1 is a cross-sectional drawing illustrating the resulting structure from the foregoing processing steps. Shown in figure 1 are
substrate 2, interlevel dielectric layer 3,adhesion layer 6,barrier layer 4 andplanarization layer 8. - The process is continued as follows:
- 6) Heat the wafer to above the melting point of tin but below, for instance, 500°C, a temperature which will not degrade lower metal layers. The wafer can be heated, for example, in an inert ambient such as in argon to 250° to 400° C for a few seconds to a few minutes. The heating beyond the melting point of tin will produce a liquid metal film. Surface tension forces will produce a completely flat tin melt surface which is planar on both local and global scales. Note that in selecting a material suitable for a planarization layer the surface tension forces must overcome the viscosity forces. Once again, for this requirement, tin is a suitable choice for the planarization layer since, for instance, at 300° C tin has a surface tension force of more than 550 mN/m and a low viscosity of 1.73 cp (similar to isopropyl alcohol). Therefore, excellent large-scale/global planarization is expected when the wafer is heated to 300°C and then cooled back to near room temperature (for tin to resolidify) as explained in the subsequent process step. Note that the wafer heating can take place in-situ during or after the tin sputter deposition or CVD-based deposition process. The heating temperature is low enough (below approximately 400°C) so that the tin does not diffuse through the underlying barrier and dielectric layers. Moreover, the metal melt has sufficiently low viscosity and large surface tension forces to extend the planar melt (molten tin) surface on a global scale.
- 7) Remove the wafer from the heated area or alternatively turn the thermal enenergy source off. This will cause the solidification of the planarized tin melt and form a globally planarized solid tin melt surface. Tin expands slightly upon solidification. This slight expansion is accommodated in the vertical direction resulting in only a slightly larger solid planarized tin thickness compared to the melt thickness.
- 8) Perform a blanket etch process such that the etch rates for tin and the ILD (as well as the thin glue and barrier layers) are similar (i.e. 1/1 selectivity - In general, the etch-back process must have a 1:1 selectivity between tin and the underlayers for instance, oxide dielectric as well as the nitride barrier and TiW or TiN adhesion/glue layers. Good etch uniformity is required). This may be accomplished with a suitable reactive ion etch (RIE) or sputter etch process. The sputter etch process for tin etch-back can be replaced with an RIE process if a suitable etch chemistry is available. The uniform blanket etch is continued until all the tin and the initial ILD surface topography are completely removed. The etch-stop level can be easily detected by using an in-situ surface reflectance sensor which detects the end-point for the etch process breaking through the lowest tin-containing regions. This will result in a globally planar ILD surface. An in-situ laser-based surface reflectance sensor can easily detect the end-point for the etch-back process. This is due to the fact that the surface reflectance will start to decrease (or change) rapidly when the etch-back process reaches the underlayer peaks by breaking through the resolidified tin layer. Figure 3 illustrates a qualitative graph of the surface reflectance R versus time t. The reflectance is measured for this case using a 1.3 or 1.55 µm wavelength large-diameter ( e.g. 1-10 mm) laser beam. A surface reflectance of R₀ is obtained at the very beginning of the etch period which begins at t₀. Time t₁ indicates the time at which the etch-back process arrives at the underlayer's highest peak, while tf indicates an optimal etch end-point detected via surface reflectance. After a time tf, fringes may exist in the reflectance signal due to dielectric etch. Consequently, global planarization occurs within a time t₁ and tf with tf shown here as representative of the most suitable etch time. The reflectance measurement process discussed here is compatible with face-up, face-down and vertical wafer processing schemes. As a result of surface reflectance use for determining the etch end-point level, it is desirable to provide a planarization layer which also offers good reflectivity. Tin is a silvery white metal while indium is silvery-white in color. Both offer good surface reflectivity. For instance, indium can be plated onto metals and evaporated onto glass to a form a mirror as good as those made with silver. Alternatively, the etch-back end-point process can use an electrical end-point instead of an optical end-point. For instance, a two-point probe may be used in order to monitor the metal sheet resistance (tin sheet resistance) in real time. Figure 4 illustrates a qualitative graph showing sheet resistance measured in ohms per square versus etch time t. The sheet resistance measurement can be taken from 2-point probe data. Time t₀ represents the etch-back start time while time tf represents the etch-back end-point or stop time. Figure 5 is a cross-sectional drawing similar to figure 1, with the exception that etch
line 10 illustrates the etch back end-point level (shown as dielectric surface 1 (in figure 5). Figure 5 illustrates the resulting structure after the foregoing processing steps. Note that a planar surface 12 which extends globally now exists. If necessary a dielectric deposition step can be performed to make the ILD (the globally planar ILD) thicker after the tin etch-back step. The remaining process steps proceed as follows: - 9) Proceed with the fabrication of the metal level.
- 10) Deposit an interlevel dielectric (ILD).
- 11) Repeat steps 3 through 8 to complete the next planarization level.
- 12) Repeat the process sequence until all the metal levels desired are fabricated.
- Note that the entire sequence of planarization steps (tin sputter deposition or tin CVD, wafer heating/tin melting, wafer cooling/ tin solidification, tin etch-back) can be performed in-situ within a single PVD or CVD chamber.
- The deposition process of the planarization layer can be performed while the wafer is heated to above the melting point of tin (e.g. between 232°C and 400°C). This will result in formation of globally planar tin melt during the deposition. As a result, the two steps of tin deposition and melt resolidification can be performed in a single process step.
- Although the invention has been described in detail herein with reference to its preferred embodiments and certain described alternatives, it is to be understood that this description is by way of example only, and it is not to be construed in a limiting sense. It is further understood that numerous changes in the details of the embodiments of the invention, and additional embodiments of the invention, will be apparent to, and may be made by persons of ordinary skill in the art having reference to this description. For instance, note that the adhesion/buffer layer may not always be necessary. Although tin was specifically cited as the preferred choice for the planarization layer, other materials meeting the guidelines set forth above can be easily substituted. For instance, indium or bismuth can be used. Additionally note that alloys of the metals listed above can be used. Further, the foregoing disclosed invention is fully compatible with back-end device processing. It is contemplated that all such changes and additional embodiments are within the spirit and true scope of the invention as claimed below.
METAL | MELTING PT. (°C) | BOILING PT. (°C) |
Indium | 156.61 | 2080 @ 760 Torr |
Bismuth | 271.3 | 1560 @ 760 Torr |
Tin | 231.97 | 2270 @ 760 Torr |
Claims (19)
- A method of planarizing a structure lying on a substrate comprising:
depositing a disposable planarization layer which is in solid form at room temperature;
forming a liquid melt from said planarization layer over the substrate so as to form a planar liquid melt surface;
solidifying said melt so as to form a planar solid layer;
etching back said planar solid layer to a predetermined level on said structure. - A method as recited in claim 1 wherein said liquid melt is formed from a material having greater surface tension forces than forces of viscosity.
- A method as recited in claim 1 wherein said substrate is formed of semiconductor material.
- A method of planarizing an interlevel dielectric layer on a substrate comprising:
placing an interlevel dielectric layer over said substrate;
placing an adhesion layer over said interlevel dielectric;
placing a planarization layer over said adhesion layer;
melting, planarizing and resolidifying said planarization layer via heating and cooling said substrate; and
etching-back said planarization layer into said interlevel dielectric layer so as to form a planar surface on said interlevel dielectric layer. - A method as recited in claim 1 wherein said etch-back is performed with an etch process including a 1-to-1 etchant selectivity as between said planarization layer and said interlevel dielectric layer.
- A method as recited in claim 4 wherein a barrier layer is placed on said interlevel dielectric and said adhesion layer is placed over said barrier layer.
- A method as recited in claim 4 wherein said interlevel dielectric is deposited over said substrate.
- A method as recited in claim 4 wherein said interlevel dielectric layer comprises a dielectric selected from the group consisting of phosophosilicate glass or borophosphosilicate glass, undoped oxide or a combination thereof..
- A method as recited in claim 4 wherein said adhesion layer comprises a material selected from the group consisting of titanium, silicon or aluminium.
- A method as recited in claim 9 wherein said adhesion layer comprises a material selected from the group consisting of TiW or TiN.
- A method as recited in claim 6 wherein said barrier layer comprises Si₃N₄ or silicon oxynitride.
- A method as recited in claim 4 wherein said planarization layer is selected from the group consisting of tin, tin alloy, bismuth, bismuth alloy, indium, indium alloy, or a combination thereof.
- A method as recited in claim 6 wherein said barrier layer is a plasma deposited silicon nitride material.
- A method as recited in claim 4 wherein said adhesion layer serves as a buffer against contaminants to said substrate.
- A method as recited in claim 4 wherein said adhesion layer is deposited according to a method selected from the group consisting of physical-vapor deposition or chemical-vapor deposition.
- A method as recited in claim 4 wherein said planarization layer is deposited over said adhesion layer according to a physical-deposition process or chemical-deposition process or an evaporation or plating process.
- A method of planarizing an interlevel dielectric layer on a substrate comprising:
placing an interlevel dielectric layer over said substrate;
placing an adhesion layer over said interlevel dielectric;
placing a planarization layer over said adhesion layer;
melting, planarizing, and resolidifying said planarization layer via heating and cooling said substrate;
etching-back said planarization layer into said interlevel dielectric layer until detecting an etch-back end-point level. - A method as recited in claim 17 wherein said etch-back end-point level is detected using a method of measuring surface reflectance.
- A method as recited in claim 17 wherein said etch-back end-point is detected using a method of measuring electrical sheet resistance.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US816458 | 1991-12-31 | ||
US07/816,458 US5284804A (en) | 1991-12-31 | 1991-12-31 | Global planarization process |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0549994A2 true EP0549994A2 (en) | 1993-07-07 |
EP0549994A3 EP0549994A3 (en) | 1993-07-28 |
EP0549994B1 EP0549994B1 (en) | 1996-07-17 |
Family
ID=25220681
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92121777A Expired - Lifetime EP0549994B1 (en) | 1991-12-31 | 1992-12-22 | Global planarization process |
Country Status (5)
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US (1) | US5284804A (en) |
EP (1) | EP0549994B1 (en) |
JP (1) | JP3361847B2 (en) |
DE (1) | DE69212295T2 (en) |
TW (1) | TW256934B (en) |
Cited By (1)
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EP1182273A2 (en) * | 2000-08-24 | 2002-02-27 | Applied Materials, Inc. | Gas chemistry cycling to achieve high aspect ratio gapfill with hdp-cvd |
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US5354695A (en) * | 1992-04-08 | 1994-10-11 | Leedy Glenn J | Membrane dielectric isolation IC fabrication |
US6714625B1 (en) * | 1992-04-08 | 2004-03-30 | Elm Technology Corporation | Lithography device for semiconductor circuit pattern generation |
US6355553B1 (en) * | 1992-07-21 | 2002-03-12 | Sony Corporation | Method of forming a metal plug in a contact hole |
US5372974A (en) * | 1993-03-19 | 1994-12-13 | Micron Semiconductor, Inc. | Approach to avoid buckling in BPSG by using an intermediate barrier layer |
US6690044B1 (en) | 1993-03-19 | 2004-02-10 | Micron Technology, Inc. | Approach to avoid buckling BPSG by using an intermediate barrier layer |
US5532188A (en) * | 1994-03-30 | 1996-07-02 | Wright; Peter J. | Global planarization of multiple layers |
KR0159388B1 (en) * | 1995-09-30 | 1999-02-01 | 배순훈 | Method for planarization |
US5885900A (en) * | 1995-11-07 | 1999-03-23 | Lucent Technologies Inc. | Method of global planarization in fabricating integrated circuit devices |
US5837603A (en) * | 1996-05-08 | 1998-11-17 | Harris Corporation | Planarization method by use of particle dispersion and subsequent thermal flow |
US6551857B2 (en) | 1997-04-04 | 2003-04-22 | Elm Technology Corporation | Three dimensional structure integrated circuits |
US5915167A (en) * | 1997-04-04 | 1999-06-22 | Elm Technology Corporation | Three dimensional structure memory |
JP2001516970A (en) * | 1997-09-18 | 2001-10-02 | シーブイシー プロダクツ、インコーポレイテッド | Method and apparatus for interconnect fabrication of high performance integrated circuits |
WO2004015764A2 (en) * | 2002-08-08 | 2004-02-19 | Leedy Glenn J | Vertical system integration |
KR100587635B1 (en) * | 2003-06-10 | 2006-06-07 | 주식회사 하이닉스반도체 | Method for fabrication of semiconductor device |
US20090074962A1 (en) * | 2007-09-14 | 2009-03-19 | Asml Netherlands B.V. | Method for the protection of an optical element of a lithographic apparatus and device manufacturing method |
JP2014053502A (en) * | 2012-09-07 | 2014-03-20 | Toshiba Corp | Manufacturing method for semiconductor device |
JP2023002853A (en) * | 2019-12-12 | 2023-01-11 | Agc株式会社 | Laminated substrate and method for manufacturing the same |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1182273A2 (en) * | 2000-08-24 | 2002-02-27 | Applied Materials, Inc. | Gas chemistry cycling to achieve high aspect ratio gapfill with hdp-cvd |
EP1182273A3 (en) * | 2000-08-24 | 2004-01-07 | Applied Materials, Inc. | Gas chemistry cycling to achieve high aspect ratio gapfill with hdp-cvd |
US7052552B2 (en) | 2000-08-24 | 2006-05-30 | Applied Materials | Gas chemistry cycling to achieve high aspect ratio gapfill with HDP-CVD |
KR100817356B1 (en) * | 2000-08-24 | 2008-03-27 | 어플라이드 머티어리얼스, 인코포레이티드 | Gas chemistry cycling to achieve high aspect ratio gapfill with hdp-cvd |
Also Published As
Publication number | Publication date |
---|---|
JP3361847B2 (en) | 2003-01-07 |
TW256934B (en) | 1995-09-11 |
EP0549994B1 (en) | 1996-07-17 |
US5284804A (en) | 1994-02-08 |
DE69212295T2 (en) | 1997-02-06 |
JPH06120180A (en) | 1994-04-28 |
DE69212295D1 (en) | 1996-08-22 |
EP0549994A3 (en) | 1993-07-28 |
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